2017
DOI: 10.1016/j.jns.2017.02.001
|View full text |Cite
|
Sign up to set email alerts
|

Association between gene polymorphism and depression in Parkinson's disease: A case-control study

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
13
0

Year Published

2017
2017
2024
2024

Publication Types

Select...
7
2

Relationship

0
9

Authors

Journals

citations
Cited by 19 publications
(13 citation statements)
references
References 29 publications
0
13
0
Order By: Relevance
“…On the other hand, Ragab and colleagues found the prevalence at 47.5% [27]. Across literature, several studies [7,[28][29][30][31] found the prevalence of depression in PD was ranging from 32.6 to 41%. A systematic review conducted by Reijnders et al reported that 17% and 22% of PD patients had MDD and minor depression, respectively [32].…”
Section: Discussionmentioning
confidence: 99%
“…On the other hand, Ragab and colleagues found the prevalence at 47.5% [27]. Across literature, several studies [7,[28][29][30][31] found the prevalence of depression in PD was ranging from 32.6 to 41%. A systematic review conducted by Reijnders et al reported that 17% and 22% of PD patients had MDD and minor depression, respectively [32].…”
Section: Discussionmentioning
confidence: 99%
“…Interestingly, serotoninergic neurons are progressively lost in PD, which is implicated both in motor and non-motor manifestations of PD [72]. Moreover, polymorphisms in TPH2 are associated with addictive behaviors [73] and depression [74] in PD patients. Additionally, Tph2 KO mice, which have serotonin deficiency, present with systemic oxidative stress and lipidomic abnormalities [75], and swallowing dysfunction [76].…”
Section: Discussionmentioning
confidence: 99%
“…BDNF (rs6265) variant has been associated with depression in people with PD, after accounting for the effects of potential confounders such as gender, disease progression and motor symptoms (p = 0.046) (Cagni et al, 2017). TEF TT genotype (Hua et al, 2012), CRY1 CC genotype (Hua et al, 2012), SLC6A15 (rs1545843) (Zheng et al, 2017) and TPH2 (rs78162420) (Zheng et al, 2017) have been associated with depression in people with PD, and these findings have not been replicated so far. Moreover, people with PD carrying SNCA Rep1 (CA)12/12 genotype reportedly has a reduced risk of depression (p = 0.02) (Dan et al, 2016).…”
Section: Supplementary Informationmentioning
confidence: 99%
“…Fourteen studies studied PD service users, who are carriers of LRRK2 variants (rs34637584, rs33939927, rs11564148 and rs34778348). Other genes that have been investigated included SNCA (Zheng et al, 2017), APOE, BDNF (rs6265), SLC6A4, COMT (Val158Met) and MAPT. Only 26 (60.5%) included studies have had sample sizes above 100.…”
Section: Fig 1 Presents the Preferred Reporting Items For Systematicmentioning
confidence: 99%